FDAClass IIAugust 20, 2014

VITROS¿ Immunodiagnostic Products CA 19-9 Calibrators recall

VITROS¿ Immunodiagnostic Products CA 19-9 Calibrators and Reagent Packs, Lot 1320 VITROS¿ CA 19-9 Reagent Packs are used on VITROS¿ ECi/ECiQ…

Why was VITROS¿ Immunodiagnostic Products CA 19-9 Calibrators recalled?

Customers may receive positively biased results when using VITROS¿ Immunodiagnostic Products CA 19-9 Total Reagent Packs, Lot 1320 and VITROS¿ CA 19-9 Calibrators, Lot 1320 on the VITROS ECi/ECiQ Immunodiagnostic Systems, the VITROS 3600 Immunodiagnostic System and the VITROS 5600 Integrated System. There is an unexpected observed change in CA 19-9 Calibrators, Lot 1320 calibrator values.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot 1320, Product code: 6800035 and 6800040

Product
VITROS¿ Immunodiagnostic Products CA 19-9 Calibrators and Reagent Packs, Lot 1320 VITROS¿ CA 19-9 Reagent Packs are used on VITROS¿ ECi/ECiQ…
Recalling firm
ORTHO-CLINICAL DIAGNOSTICS
Quantity
475
Distribution
Worldwide Distribution - USA (nationwide) and Internationally to France and Japan
Recall date
August 20, 2014
Classification
Class II
Status
Terminated
Agency
FDA (device)
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